Neurofibromatosis type 1, hyperparathyroidism, and osteosarcoma: interplay?
β Scribed by Udi Cinamon; Ilana Avinoach; Moshe Harell
- Book ID
- 106082371
- Publisher
- Springer-Verlag
- Year
- 2002
- Tongue
- English
- Weight
- 210 KB
- Volume
- 259
- Category
- Article
- ISSN
- 0302-9530
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π SIMILAR VOLUMES
Neurofibromatosis 1 (NF1) is an autosomal dominant neurocutaneous disorder with an incidence of approximately 1 in 4000. Cognitive deficits and academic learning difficulties are the most common neurological 'complication' of NF1 in childhood and can be responsible for significant lifetime morbidity
Neurofibromatosis '&pe 1 (NF-1) is an autosomal dominant condition which has markedly variable clinical expression, with manifestations ranging from mild cutaneous lesions to severe orthopedic complications and functional impairment. The current obstetrical literature indicates that women with NF-1
The prevalence of neurofibromatosis type 1 (NF1) is about 1/3,000. There are no known ethnic groups in which NF1 does not occur or is unusually common. The prevalence is somewhat higher in young children than in adults, a difference that probably results at least in part from the early death of some
Growth abnormalities such as macrocephaly and short stature have been described and are considered a consistent finding in neurofibromatosis type 1 (NF1), one of the most common autosomal dominant disorders in man. We present here a clinical study on the growth profile of a sample of NF1 patients co